EP3612376B1 - Method of producing agglomerates for inclusion in a composite material - Google Patents

Method of producing agglomerates for inclusion in a composite material Download PDF

Info

Publication number
EP3612376B1
EP3612376B1 EP18721091.9A EP18721091A EP3612376B1 EP 3612376 B1 EP3612376 B1 EP 3612376B1 EP 18721091 A EP18721091 A EP 18721091A EP 3612376 B1 EP3612376 B1 EP 3612376B1
Authority
EP
European Patent Office
Prior art keywords
agglomerates
composite material
producing
semi
electrically conductive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP18721091.9A
Other languages
German (de)
French (fr)
Other versions
EP3612376A1 (en
Inventor
Sarah Jessica DEMPSEY
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Peratech Holdco Ltd
Original Assignee
Peratech Holdco Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Peratech Holdco Ltd filed Critical Peratech Holdco Ltd
Publication of EP3612376A1 publication Critical patent/EP3612376A1/en
Application granted granted Critical
Publication of EP3612376B1 publication Critical patent/EP3612376B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/205Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
    • C08J3/21Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
    • C08J3/212Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase and solid additives
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01CRESISTORS
    • H01C10/00Adjustable resistors
    • H01C10/10Adjustable resistors adjustable by mechanical pressure or force
    • H01C10/106Adjustable resistors adjustable by mechanical pressure or force on resistive material dispersed in an elastic material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C67/00Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
    • B29C67/24Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00 characterised by the choice of material
    • B29C67/242Moulding mineral aggregates bonded with resin, e.g. resin concrete
    • B29C67/243Moulding mineral aggregates bonded with resin, e.g. resin concrete for making articles of definite length
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F23/00Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
    • B01F23/50Mixing liquids with solids
    • B01F23/51Methods thereof
    • B01F23/511Methods thereof characterised by the composition of the liquids or solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F23/00Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
    • B01F23/50Mixing liquids with solids
    • B01F23/53Mixing liquids with solids using driven stirrers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F23/00Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
    • B01F23/80After-treatment of the mixture
    • B01F23/811Heating the mixture
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F29/00Mixers with rotating receptacles
    • B01F29/15Use of centrifuges for mixing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B15/00Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
    • B29B15/08Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
    • B29B15/10Coating or impregnating independently of the moulding or shaping step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/16Solid spheres
    • C08K7/18Solid spheres inorganic
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/041Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
    • G06F3/0414Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means using force sensing means to determine a position
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/041Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
    • G06F3/045Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means using resistive elements, e.g. a single continuous surface or two parallel surfaces put in contact
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/22Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F2101/00Mixing characterised by the nature of the mixed materials or by the application field
    • B01F2101/2805Mixing plastics, polymer material ingredients, monomers or oligomers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01FMIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F2215/00Auxiliary or complementary information in relation with mixing
    • B01F2215/04Technical information in relation with mixing
    • B01F2215/0413Numerical information
    • B01F2215/0436Operational information
    • B01F2215/0459Numerical values of dimensionless numbers, i.e. Re, Pr, Nu, transfer coefficients
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2505/00Use of metals, their alloys or their compounds, as filler
    • B29K2505/06Tin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0003Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular electrical or magnetic properties, e.g. piezoelectric
    • B29K2995/0005Conductive
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2300/00Characterised by the use of unspecified polymers
    • C08J2300/24Thermosetting resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2483/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
    • C08J2483/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2231Oxides; Hydroxides of metals of tin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/001Conductive additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/005Additives being defined by their particle size in general
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives

Definitions

  • the present invention relates to a method of producing a plurality of agglomerates for inclusion in an electrically responsive composite material.
  • User input devices are known that are substantially flat and are responsive to movement of a stylus or finger in an xy plane, and in some cases, also sensitive to pressure applied in the z dimension.
  • touch screens When incorporated into touch screens, it has previously proved difficult to produce transparent touch screens which operate in both the xy plane and the z dimension, this problem being previously identified in the applicant's patent EP 2 689 431 .
  • EP 2 689 431 provides a pressure sensitive composite material which comprises a plurality of agglomerates dispersed within a carrier layer.
  • these agglomerates are spontaneously formed by a process of mixing conductive or semi-conductive particles in combination with a polymeric material to produce the composite material in question.
  • the conductive or semi-conductive particles combine with other conductive or semi-conductive particles to form the agglomerates within the carrier layer.
  • the formed agglomerates are dependent on the mixing process of the composite material and require a limitation of hyper-dispersant levels so that the agglomerates can form.
  • the resulting agglomerates are often irregular with varying mechanical and electrical properties and the composite material often includes small agglomerates which provide limited conduction through the carrier layer and optical haze through an otherwise transparent or translucent material.
  • the invention is directed to a method of producing a plurality of agglomerates for inclusion in an electrically responsive composite material, comprising the steps of: obtaining a plurality of electrically conductive or semi-conductive particles; mixing said plurality of electrically conductive or semi-conductive particles in a centrifugal mixer, said mixing step comprising operating said centrifugal mixer at a Froude number of between 220 and 1100; and adhering said plurality of electrically conductive or semi-conductive particles by adding a granulation binder and mixing said granulation binder with said plurality of electrically conductive or semi-conductive particles to form a plurality of agglomerates; wherein each said step of obtaining, mixing and adhering said electrically conductive or semi-conductive particles pre-forms said plurality of agglomerates prior to introduction of said plurality of agglomerates into said electrically responsive composite material.
  • Electrically responsive composite material 101 is illustrated in Figure 1 .
  • Electrically responsive composite material 101 is suitable for applying to a suitable substrate and can thus be incorporated into an electronic device such as a touch screen.
  • Composite material 101 comprises a plurality of agglomerates 102 which are dispersed within a carrier layer 103 .
  • Carrier layer 103 comprises a polymer binder which can be crosslinkable, solvent-based, thermally or uv-curable.
  • the polymer binder may also be opaque, translucent or substantially transparent and remains such after cross-linking, solvent evaporation or curing.
  • Each of the agglomerates 102 comprise a plurality of electrically conductive or semi-conductive particles 103 which are adhered together to form the agglomerates 102 .
  • the agglomerates are pre-formed and then dispersed within the carrier layer in the manner of Figure 1 .
  • Pre-formed is used throughout this specification to indicate that the agglomerates are produced by combining a plurality of electrically conductive or semi-conductive particles separately and before combining the agglomerates with the carrier layer.
  • agglomerate is used throughout the specification to refer to a granular particle which has been formed from a plurality of electrically conductive or semi-conductive particles though a granulation method and which is able to provide conduction through the agglomerate itself.
  • each individual agglomerate can then be combined with appropriate carrier binders to produce conductive composite materials.
  • the size and dispersion of the agglomerates is such as to render them invisible to an unaided eye.
  • the size of the agglomerates is such that a thin coating of the electrically responsive composite material appears optically substantially the same as without the addition of the filler particles.
  • the composite material as a whole may take the optical appearance of the polymer binder.
  • Figure 2 shows a schematic of a method of producing a plurality of agglomerates 102 which are suitable for inclusion in an electrically responsive composite material, such as electrically composite material 101 as previously described in Figure 1 . It is noted that the schematic is diagrammatical in nature and therefore not to scale.
  • a plurality of electrically conductive or semi-conductive particles 201 are obtained and are placed into a granulation vessel 202 .
  • a granulation binder 203 is also added into the granulation vessel 202 .
  • the granulation vessel 202 is configured to perform a mixing process so that the plurality of electrically conductive or semi-conductive particles 201 adhere to each other during the mixing process.
  • particles 201 adhere together due to the presence of binder 203 .
  • the plurality of agglomerates 102 comprise a plurality of electrically conductive or semi-conductive particles 201 which have been adhered together by the mixing process performed by the granulation vessel 202 .
  • the ratio of the plurality of electrically conductive or semi-conductive particles 201 to granulation binder 203 is 10:1 weight/weight.
  • the amount of granulation binder used to adhere the particles together is relatively small compared to the amount of particles which form each agglomerate.
  • alternative ratios which allow the electrically conductive and/or semi-conductive particles to adhere to each other are used.
  • the conductive particles comprise antimony doped tin oxide particles. These are illustrated as spherical particles; however, it is appreciated that, in alternative embodiments, the particles are acicular (or needle shaped).
  • the electrically conductive or semi-conductive particles typically have a largest dimension of between ten (10) and one hundred (100) nanometres (nm).
  • granulation binder 203 comprises a silicone liquid binder, and in particular, comprises a two-part translucent high consistency rubber of which the main constituent is polydimethylsiloxane (PDMS).
  • the granulation binder comprises a carbon-based (organic) binder such as an alcohol/petrol resistant (APR) varnish.
  • the granulation binder comprises a water-based binder, for example a transparent screen-printable ink containing no organic solvent.
  • other suitable granulation binders may be used.
  • Granulation vessel 202 is configured to mix the particles and granulation binder at relatively high energies so as to produce agglomerates which do not break up easily.
  • the granulation vessel is a centrifugal mixer.
  • the centrifugal mixer has a dual axis of rotation, such as a SpeedMixerTM DAC 150.1 FVZ dual asymmetric centrifugal laboratory mixer as will be described in further detail with respect to Figure 3 .
  • FIG. 3 A schematic representation of a granulation vessel in the form of a dual axis centrifugal mixer which is suitable for performing a granulation process in accordance with the present invention is shown with respect to Figure 3 .
  • the granulation vessel of Figure 2 can be any other suitable vessel which is able to produce suitable agglomerates of the type described herein, with Figure 3 providing a suitable example which is able to achieve the agglomerates herein described.
  • a sample container 301 is provided into which the plurality of electrically conductive or semi-conductive particles 201 can be added along with the corresponding granulation binder 203 .
  • Sample container 301 is positioned at one end of a rotational arm 302 which is inclined at an angle 303 to the horizontal 304 about the cylindrical vessel having a radius 305 .
  • angle 303 is set at forty degrees (40°) to the horizontal 304 , with the radius being eighty millimetres (80mm).
  • rotational arm 302 is rotated about a central rotation axis 306 , so that the sample container 301 , due to its position at the end of rotational arm 302 , moves in a circular manner in the direction of arrows 307 .
  • the dual axis centrifugal mixer 202 is further configured to rotate sample container 301 about a secondary rotation axis 308 , in an opposed direction to that of the central rotation 306 . This is indicated by the arrow 309 .
  • a dual asymmetric centrifuge of this type is advantageous as it promotes rapid homogenisation of the sample in the container and reduces air bubbles in the sample. This is due to the high acceleration and opposing centripetal forces imposed by the opposing axes.
  • this type of mixer is not used for granulation processes, but for mixing two separate liquids together. The applicant has found, however, that a dual axis mixer of this type produces suitable agglomerates for use in an electrically responsive composite material.
  • this particular granulation vessel is that parameters such as the radius of rotation and speed of rotation can be varied to provide suitable results.
  • the speed of rotation is relatively high which produces a high Froude number as will described in detail with respect to Figure 4 .
  • the dual axis centrifugal mixer as described in respect of Figure 3 is configured to operate at a high energy having a Froude number of between 220 and 1100.
  • the Froude number of a granulator is a measure of the centripetal acceleration acting on the sample in the sample container as a ratio of the gravitational acceleration. It is therefore defined by the square of the angular velocity multiplied by the characteristic radius of the granulation vessel and divided by the gravitational acceleration. Control of the Froude number of the granulation vessel in use can be used to compare the energy of granulation imparted onto the particles.
  • Figure 4 illustrates a graph of Froude number against the rotational speed about the central axis 306 in revolutions per minute (rpm).
  • Line 401 shows the variation in Froude number with increased rotational speed.
  • the centrifugal mixer of Figure 3 operates at a rotational speed of between 1000 and 3500 rpm which produces a corresponding Froude number of between 220 and 1100.
  • a Froude number of 1096 has been measured.
  • a Froude number of between 229 and 1095 corresponds to a rotational speed of between 1600 and 3500 rpm.
  • FIG. 5 a graph of rotational speed (revolutions per minute - rpm) against the granulation time (minutes) is shown in Figure 5 .
  • the graph described in respect of Figure 5 is illustrative of the process by which the agglomerates are formed through granulation.
  • the granulation process involves a nucleation phase which results in relatively small agglomerates. This phase is then followed by a rapid growth phase in which an increased number of conductive particles join or stick to the forming agglomerate.
  • the graph of Figure 5 illustrates how the timing of these phases can be controlled to result in agglomerates of different properties.
  • the graph illustrates three regions, 501 , 502 and 503 indicating the relationship between the two parameters and the corresponding size of agglomerates produced.
  • region 501 agglomerates were produced of sizes having a greatest dimension of less than ten micrometres (10 ⁇ m). Thus, in this region, the agglomerates produced are relatively small.
  • region 502 the agglomerates larger, surface-smooth agglomerates are produced which typically have a largest dimension of between twenty and forty micrometres (20-40 ⁇ m).
  • the agglomerates are larger and may be more than forty micrometres (40 ⁇ m) across their largest dimension.
  • Agglomerates in region 503 have been noted to include a plurality of indentations on their surface which provides an appearance similar to a golf-ball.
  • the agglomerates have a largest dimension of between four and twenty micrometres (4-20 ⁇ m) and preferably between four and ten micrometres (4-10 ⁇ m) and typically have a smooth surface and relatively consistent overall size.
  • the agglomerates produced are larger and have indentations on their surface, as will be described in further detail in Figure 6 .
  • Example agglomerates in accordance with the present invention are shown in Figure 6 .
  • Agglomerates 601 and 602 have been produced by the method described previously in respect of Figure 2 .
  • agglomerates 601 and 602 include a plurality of indentations, such as indentations 603 and 604 on surface 605 of agglomerate 601 .
  • these agglomerates have a relatively large surface area compared to agglomerates having a smooth surface.
  • the largest dimension of the agglomerates is typically between twenty and forty micrometres (20-40 ⁇ m); however, agglomerates of over forty micrometres (40 ⁇ m) can be produced in this manner.
  • a method of producing a plurality of agglomerates of the types previously described herein is shown in diagrammatic form in Figure 7 .
  • electrically conductive or semi-conductive particles 201 are obtained.
  • the particles 201 comprise antimony doped tin oxide spherical particles.
  • the antimony doped tin oxide particles are acicular or needle-shaped. Each particle typically has a largest dimension of between ten and one hundred nanometres (10-100 nm).
  • a granulation binder 203 is obtained.
  • the granulation binder is in the form of a liquid and is typically a silicone liquid binder such as one which comprises a two-part translucent high consistency rubber of which the main constituent is polydimethylsiloxane (PDMS).
  • granulation binder 203 comprises a carbon-based (organic) binder such as an alcohol/petrol resistant (APR) varnish.
  • the granulation binder comprises a water-based binder, for example a transparent screen-printable ink containing no organic solvent.
  • the particles and granulation binder are introduced into a granulation vessel in the manner of Figure 2 and undergo a mixing process which adheres the particles together to produce agglomerates at step 703 .
  • the process of mixing and adhering the particles can be varied as described above in order to obtain agglomerates having particular properties, such as varied sizes, shapes, or porosity, which is affected by the granulation time.
  • the agglomerates are then removed from the granulation vessel and undergo a curing process at step 704 .
  • this involves placing the agglomerates into a suitable oven and applying a heating process to the agglomerates.
  • the agglomerates undergo a further size selection process which ensures that each said agglomerate is within a predetermined size range.
  • the agglomerates are sieved at twenty micrometres (20 ⁇ m) so maintain the agglomerates as being smaller than twenty micrometres (20 ⁇ m). This assists in ensuring that the agglomerates are of a suitable size for any future applications, such as the inclusion into an electrically responsive composite material. It is appreciated that other size selection processes may be utilised that allow the agglomerates to be sorted in accordance with their future applications.
  • the plurality of agglomerates are then able to be used in the production of a composite material, which in turn can form part of a touch screen or other electronic device.
  • the plurality of agglomerates are introduced into a liquid carrier and mixed into the liquid carrier to produce the composite material which will now be described with respect to Figure 8 .
  • the plurality of agglomerates ( 802 , 803 ) have been introduced into a liquid carrier which has been solidified to produce a solidified polymeric material.
  • the carrier layer comprises any suitable liquid carrier which comprises a component capable of solidifying to produce a solidified polymeric material and in order to produce the composite material, the agglomerates are introduced into the liquid carrier and mixed to disperse the agglomerates within the liquid carrier before solidification takes place.
  • the resultant carrier layer 804 has a length and a width and a thickness 805 which is relatively small compared to the width.
  • the thickness 805 is between four and six micrometres (4-6 ⁇ m).
  • the plurality of agglomerates ( 802 , 803 ) have a largest dimension of between four and twenty micrometres (4-20 ⁇ m), but in the embodiment, the largest dimension is typically between four and ten micrometres (4-10 ⁇ m).
  • the thickness 805 of carrier layer 804 is smaller than the largest dimension of each agglomerate.
  • the agglomerates have a largest dimension of between eight and ten micrometres (8-10 ⁇ m) for a carrier layer thickness of six micrometres (6 ⁇ m).
  • the agglomerates protrude slightly from the solidified carrier layer so that they are able to provide a conductive path.
  • the agglomerates In contrast to previous method of manufacture, because the agglomerates have been pre-formed prior to their inclusion into the liquid binder, the agglomerates are able to be provided with consistent properties, both mechanical and electrical. Thus, this reduces the number of particles which do not form usable agglomerates, for example, those which are too small to provide a conductive path through the carrier layer.
  • FIG. 9 A diagrammatic illustration of conduction paths through a composite material in accordance with the invention is shown in Figure 9 .
  • the composite material has been incorporated into a touch screen having a deformable electrode of indium tin oxide (ITO) 901 and a rigid electrode of indium tin oxide (ITO) 902 .
  • a composite material 903 is sandwiched between the two electrodes 901 and 902 , which comprises a solidified polymeric insulating carrier layer 904 and a plurality of agglomerates, such as agglomerate 905 .
  • agglomerate 905 When a low force is applied to deformable electrode 901 , indicated by arrow 906 , agglomerate 905 is brought into contact with electrode 901 which creates a limited conduction path indicated by arrow 907 , as shown in Figure 9A .
  • a larger force indicated by arrow 908
  • contact is made, not only with agglomerate 905 , but also agglomerates 909 and 910 .
  • Conduction paths are illustrated by arrows 911 , 912 and 913 .
  • the agglomerates themselves may exhibit a pressure sensitive electrical resistance, such that with a higher applied force, there is also a further increase in conduction for this reason.
  • a graph of force against resistance for samples corresponding to composite materials of the type previously manufactured in accordance with the applicant's patent EP 2 689 431 , and composite materials in accordance with the present invention is shown in Figure 10 .
  • Line 1001 shows the force-resistance response of a sample in accordance with the present invention, where the agglomerates have been pre-formed.
  • Line 1002 shows the force-resistance response of a sample in accordance with the previously known method which creates agglomerates spontaneously.
  • the agglomerates were pre-formed using a centrifugal mixer as described with respect to Figure 3 , at a rotational speed of 2000 rpm for four minutes.
  • the present invention produces a less sensitive force-resistance response at low forces, meaning the composite material operates less like a switch than conventional methods. This can be useful in digital on/off applications. Visible light transmission is also improved as there is reduced haze from lack of non-conducting smaller agglomerates.
  • the present invention not only provides a suitable method for controlling the parameters of the agglomerates to suit a particular application, but also provides characteristics that are not provided by spontaneous agglomerate formation.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Mechanical Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Theoretical Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Structural Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • General Physics & Mathematics (AREA)
  • Human Computer Interaction (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates to a method of producing a plurality of agglomerates for inclusion in an electrically responsive composite material.
  • User input devices are known that are substantially flat and are responsive to movement of a stylus or finger in an xy plane, and in some cases, also sensitive to pressure applied in the z dimension. When incorporated into touch screens, it has previously proved difficult to produce transparent touch screens which operate in both the xy plane and the z dimension, this problem being previously identified in the applicant's patent EP 2 689 431 .
  • EP 2 689 431 provides a pressure sensitive composite material which comprises a plurality of agglomerates dispersed within a carrier layer. In manufacture, these agglomerates are spontaneously formed by a process of mixing conductive or semi-conductive particles in combination with a polymeric material to produce the composite material in question. During mixing, the conductive or semi-conductive particles combine with other conductive or semi-conductive particles to form the agglomerates within the carrier layer. Thus, the formed agglomerates are dependent on the mixing process of the composite material and require a limitation of hyper-dispersant levels so that the agglomerates can form. The resulting agglomerates are often irregular with varying mechanical and electrical properties and the composite material often includes small agglomerates which provide limited conduction through the carrier layer and optical haze through an otherwise transparent or translucent material.
  • BRIEF SUMMARY OF THE INVENTION
  • The invention is directed to a method of producing a plurality of agglomerates for inclusion in an electrically responsive composite material, comprising the steps of: obtaining a plurality of electrically conductive or semi-conductive particles; mixing said plurality of electrically conductive or semi-conductive particles in a centrifugal mixer, said mixing step comprising operating said centrifugal mixer at a Froude number of between 220 and 1100; and adhering said plurality of electrically conductive or semi-conductive particles by adding a granulation binder and mixing said granulation binder with said plurality of electrically conductive or semi-conductive particles to form a plurality of agglomerates; wherein each said step of obtaining, mixing and adhering said electrically conductive or semi-conductive particles pre-forms said plurality of agglomerates prior to introduction of said plurality of agglomerates into said electrically responsive composite material.
  • Embodiments of the invention will be described, by way of example only, with reference to the accompanying drawings. The detailed embodiments show the best mode known to the inventor and provide support for the invention as claimed. However, they are only exemplary and should not be used to interpret or limit the scope of the claims. Their purpose is to provide a teaching to those skilled in the art.
  • Components and processes distinguished by ordinal phrases such as "first" and "second" do not necessarily define an order or ranking of any sort.
  • BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
    • Figure 1 shows an electrically responsive composite material;
    • Figure 2 shows a schematic method of producing a plurality of agglomerates;
    • Figure 3 shows a schematic representation of a granulation vessel in the form of a dual axis centrifugal mixer;
    • Figure 4 shows a graph of Froude number against the rotational speed for a granulation vessel in accordance with the present invention;
    • Figure 5 shows a graph of rotational speed against the granulation time for a granulation vessel in accordance with the present invention;
    • Figure 6 shows agglomerates have a plurality of indentations on their surface;
    • Figure 7 shows a method of producing a plurality of agglomerates;
    • Figure 8 shows a composite material having a plurality of pre-formed agglomerates;
    • Figures 9A and 9B show a diagrammatic illustration of conduction paths through a composite material; and
    • Figure 10 shows a force resistance response curve for composite materials.
    DETAILED DESCRIPTION OF THE INVENTION Figure 1
  • An electrically responsive composite material 101 is illustrated in Figure 1. Electrically responsive composite material 101 is suitable for applying to a suitable substrate and can thus be incorporated into an electronic device such as a touch screen. Composite material 101 comprises a plurality of agglomerates 102 which are dispersed within a carrier layer 103. Carrier layer 103 comprises a polymer binder which can be crosslinkable, solvent-based, thermally or uv-curable. The polymer binder may also be opaque, translucent or substantially transparent and remains such after cross-linking, solvent evaporation or curing.
  • Each of the agglomerates 102 comprise a plurality of electrically conductive or semi-conductive particles 103 which are adhered together to form the agglomerates 102. In manufacture, the agglomerates are pre-formed and then dispersed within the carrier layer in the manner of Figure 1. Pre-formed is used throughout this specification to indicate that the agglomerates are produced by combining a plurality of electrically conductive or semi-conductive particles separately and before combining the agglomerates with the carrier layer. Additionally, agglomerate is used throughout the specification to refer to a granular particle which has been formed from a plurality of electrically conductive or semi-conductive particles though a granulation method and which is able to provide conduction through the agglomerate itself. Thus, each individual agglomerate can then be combined with appropriate carrier binders to produce conductive composite materials.
  • The size and dispersion of the agglomerates (shown greatly enlarged in Figure 1) is such as to render them invisible to an unaided eye. Thus, the size of the agglomerates is such that a thin coating of the electrically responsive composite material appears optically substantially the same as without the addition of the filler particles. Furthermore, as the agglomerates are dispersed within the carrier layer, the composite material as a whole may take the optical appearance of the polymer binder.
  • Figure 2
  • Figure 2 shows a schematic of a method of producing a plurality of agglomerates 102 which are suitable for inclusion in an electrically responsive composite material, such as electrically composite material 101 as previously described in Figure 1. It is noted that the schematic is diagrammatical in nature and therefore not to scale.
  • In order to produce the plurality of agglomerates 102, a plurality of electrically conductive or semi-conductive particles 201 are obtained and are placed into a granulation vessel 202. A granulation binder 203 is also added into the granulation vessel 202. The granulation vessel 202 is configured to perform a mixing process so that the plurality of electrically conductive or semi-conductive particles 201 adhere to each other during the mixing process. In the embodiment, particles 201 adhere together due to the presence of binder 203. In this way, the plurality of agglomerates 102 comprise a plurality of electrically conductive or semi-conductive particles 201 which have been adhered together by the mixing process performed by the granulation vessel 202.
  • In the embodiment, the ratio of the plurality of electrically conductive or semi-conductive particles 201 to granulation binder 203 is 10:1 weight/weight. Thus, it is appreciated that the amount of granulation binder used to adhere the particles together is relatively small compared to the amount of particles which form each agglomerate. It is further appreciated that, in alternative embodiments, alternative ratios which allow the electrically conductive and/or semi-conductive particles to adhere to each other are used.
  • In an embodiment, the conductive particles comprise antimony doped tin oxide particles. These are illustrated as spherical particles; however, it is appreciated that, in alternative embodiments, the particles are acicular (or needle shaped). The electrically conductive or semi-conductive particles typically have a largest dimension of between ten (10) and one hundred (100) nanometres (nm).
  • In an embodiment, granulation binder 203 comprises a silicone liquid binder, and in particular, comprises a two-part translucent high consistency rubber of which the main constituent is polydimethylsiloxane (PDMS). In an alternative embodiment, the granulation binder comprises a carbon-based (organic) binder such as an alcohol/petrol resistant (APR) varnish. In a further alternative embodiment, the granulation binder comprises a water-based binder, for example a transparent screen-printable ink containing no organic solvent. In still further embodiments, other suitable granulation binders may be used.
  • Granulation vessel 202 is configured to mix the particles and granulation binder at relatively high energies so as to produce agglomerates which do not break up easily. In an embodiment, the granulation vessel is a centrifugal mixer. In a particular embodiment, the centrifugal mixer has a dual axis of rotation, such as a SpeedMixer™ DAC 150.1 FVZ dual asymmetric centrifugal laboratory mixer as will be described in further detail with respect to Figure 3.
  • Figure 3
  • A schematic representation of a granulation vessel in the form of a dual axis centrifugal mixer which is suitable for performing a granulation process in accordance with the present invention is shown with respect to Figure 3. It is appreciated that the granulation vessel of Figure 2 can be any other suitable vessel which is able to produce suitable agglomerates of the type described herein, with Figure 3 providing a suitable example which is able to achieve the agglomerates herein described.
  • A sample container 301 is provided into which the plurality of electrically conductive or semi-conductive particles 201 can be added along with the corresponding granulation binder 203. Sample container 301 is positioned at one end of a rotational arm 302 which is inclined at an angle 303 to the horizontal 304 about the cylindrical vessel having a radius 305. In an embodiment, angle 303 is set at forty degrees (40°) to the horizontal 304, with the radius being eighty millimetres (80mm).
  • In use, rotational arm 302 is rotated about a central rotation axis 306, so that the sample container 301, due to its position at the end of rotational arm 302, moves in a circular manner in the direction of arrows 307. The dual axis centrifugal mixer 202 is further configured to rotate sample container 301 about a secondary rotation axis 308, in an opposed direction to that of the central rotation 306. This is indicated by the arrow 309.
  • The use of a dual asymmetric centrifuge of this type is advantageous as it promotes rapid homogenisation of the sample in the container and reduces air bubbles in the sample. This is due to the high acceleration and opposing centripetal forces imposed by the opposing axes. Traditionally, this type of mixer is not used for granulation processes, but for mixing two separate liquids together. The applicant has found, however, that a dual axis mixer of this type produces suitable agglomerates for use in an electrically responsive composite material.
  • The nature of this particular granulation vessel is that parameters such as the radius of rotation and speed of rotation can be varied to provide suitable results. In the embodiment, while the radius of rotation is maintained as a function of a particular mixer, the speed of rotation is relatively high which produces a high Froude number as will described in detail with respect to Figure 4.
  • Figure 4
  • The dual axis centrifugal mixer as described in respect of Figure 3 is configured to operate at a high energy having a Froude number of between 220 and 1100. The Froude number of a granulator is a measure of the centripetal acceleration acting on the sample in the sample container as a ratio of the gravitational acceleration. It is therefore defined by the square of the angular velocity multiplied by the characteristic radius of the granulation vessel and divided by the gravitational acceleration. Control of the Froude number of the granulation vessel in use can be used to compare the energy of granulation imparted onto the particles.
  • Figure 4 illustrates a graph of Froude number against the rotational speed about the central axis 306 in revolutions per minute (rpm). Line 401 shows the variation in Froude number with increased rotational speed. In the embodiment, the centrifugal mixer of Figure 3 operates at a rotational speed of between 1000 and 3500 rpm which produces a corresponding Froude number of between 220 and 1100. In particular, at a speed of 3500 a Froude number of 1096 has been measured. In a further embodiment, a Froude number of between 229 and 1095 corresponds to a rotational speed of between 1600 and 3500 rpm.
  • In conventional granulation vessels, it is typical for Froude numbers to range between 0.2 to around 100, and therefore the present invention imparts much higher energies into the sample (i.e. the granulation binder and electrically conductive or semi-conductive particles) than would normally be expected in a granulation process.
  • While a dual axis centrifugal mixer is described here, it is appreciated that alternative granulation vessels may be used provided that they are able to input a suitably high Froude number to provide suitable agglomerates by means of a substantially similar granulation process.
  • Figure 5
  • To further illustrate the parameters used in the method of production of pre-formed agglomerates suitable for use in an electrically responsive conductive material, a graph of rotational speed (revolutions per minute - rpm) against the granulation time (minutes) is shown in Figure 5. The graph described in respect of Figure 5 is illustrative of the process by which the agglomerates are formed through granulation. The granulation process involves a nucleation phase which results in relatively small agglomerates. This phase is then followed by a rapid growth phase in which an increased number of conductive particles join or stick to the forming agglomerate. Thus, the graph of Figure 5 illustrates how the timing of these phases can be controlled to result in agglomerates of different properties.
  • The graph illustrates three regions, 501, 502 and 503 indicating the relationship between the two parameters and the corresponding size of agglomerates produced. In region 501, agglomerates were produced of sizes having a greatest dimension of less than ten micrometres (10 µm). Thus, in this region, the agglomerates produced are relatively small. In region 502, the agglomerates larger, surface-smooth agglomerates are produced which typically have a largest dimension of between twenty and forty micrometres (20-40 µm). In region 503, the agglomerates are larger and may be more than forty micrometres (40 µm) across their largest dimension. Agglomerates in region 503 have been noted to include a plurality of indentations on their surface which provides an appearance similar to a golf-ball.
  • Thus, in an embodiment, the agglomerates have a largest dimension of between four and twenty micrometres (4-20 µm) and preferably between four and ten micrometres (4-10 µm) and typically have a smooth surface and relatively consistent overall size. However, in an alternative embodiment, the agglomerates produced are larger and have indentations on their surface, as will be described in further detail in Figure 6.
  • Figure 6
  • Example agglomerates in accordance with the present invention are shown in Figure 6. Agglomerates 601 and 602 have been produced by the method described previously in respect of Figure 2.
  • In this embodiment, the agglomerates have been produced in line with the parameters of region 3 of the graph of Figure 5. Thus, agglomerates 601 and 602 include a plurality of indentations, such as indentations 603 and 604 on surface 605 of agglomerate 601. Thus, these agglomerates have a relatively large surface area compared to agglomerates having a smooth surface. In this embodiment, the largest dimension of the agglomerates (in this case the diameter) is typically between twenty and forty micrometres (20-40 µm); however, agglomerates of over forty micrometres (40 µm) can be produced in this manner.
  • Figure 7
  • A method of producing a plurality of agglomerates of the types previously described herein is shown in diagrammatic form in Figure 7.
  • At step 701, electrically conductive or semi-conductive particles 201 are obtained. In an embodiment, the particles 201 comprise antimony doped tin oxide spherical particles. In an alternative embodiment, the antimony doped tin oxide particles are acicular or needle-shaped. Each particle typically has a largest dimension of between ten and one hundred nanometres (10-100 nm).
  • At step 702 a granulation binder 203 is obtained. The granulation binder is in the form of a liquid and is typically a silicone liquid binder such as one which comprises a two-part translucent high consistency rubber of which the main constituent is polydimethylsiloxane (PDMS). In an alternative embodiment, granulation binder 203 comprises a carbon-based (organic) binder such as an alcohol/petrol resistant (APR) varnish. In a further alternative embodiment, the granulation binder comprises a water-based binder, for example a transparent screen-printable ink containing no organic solvent.
  • The particles and granulation binder are introduced into a granulation vessel in the manner of Figure 2 and undergo a mixing process which adheres the particles together to produce agglomerates at step 703. The process of mixing and adhering the particles can be varied as described above in order to obtain agglomerates having particular properties, such as varied sizes, shapes, or porosity, which is affected by the granulation time.
  • The agglomerates are then removed from the granulation vessel and undergo a curing process at step 704. In an embodiment, this involves placing the agglomerates into a suitable oven and applying a heating process to the agglomerates.
  • At step 705, the agglomerates undergo a further size selection process which ensures that each said agglomerate is within a predetermined size range. For example, in an embodiment, the agglomerates are sieved at twenty micrometres (20 µm) so maintain the agglomerates as being smaller than twenty micrometres (20 µm). This assists in ensuring that the agglomerates are of a suitable size for any future applications, such as the inclusion into an electrically responsive composite material. It is appreciated that other size selection processes may be utilised that allow the agglomerates to be sorted in accordance with their future applications.
  • Once the plurality of agglomerates have been suitably formed as described, they are then able to be used in the production of a composite material, which in turn can form part of a touch screen or other electronic device.
  • In order to produce a composite material, the plurality of agglomerates are introduced into a liquid carrier and mixed into the liquid carrier to produce the composite material which will now be described with respect to Figure 8.
  • Figure 8
  • A composite material 801 having a plurality of agglomerates, such as agglomerates 802 and 803, which have been pre-formed by the method herein described, is shown in Figure 8.
  • The plurality of agglomerates (802, 803) have been introduced into a liquid carrier which has been solidified to produce a solidified polymeric material. In an embodiment, the carrier layer comprises any suitable liquid carrier which comprises a component capable of solidifying to produce a solidified polymeric material and in order to produce the composite material, the agglomerates are introduced into the liquid carrier and mixed to disperse the agglomerates within the liquid carrier before solidification takes place.
  • The resultant carrier layer 804 has a length and a width and a thickness 805 which is relatively small compared to the width. In the embodiment, the thickness 805 is between four and six micrometres (4-6 µm).
  • The plurality of agglomerates (802, 803) have a largest dimension of between four and twenty micrometres (4-20 µm), but in the embodiment, the largest dimension is typically between four and ten micrometres (4-10 µm). In particular, the thickness 805 of carrier layer 804 is smaller than the largest dimension of each agglomerate. For example, the agglomerates have a largest dimension of between eight and ten micrometres (8-10 µm) for a carrier layer thickness of six micrometres (6 µm). Thus, in this way, the agglomerates protrude slightly from the solidified carrier layer so that they are able to provide a conductive path.
  • In contrast to previous method of manufacture, because the agglomerates have been pre-formed prior to their inclusion into the liquid binder, the agglomerates are able to be provided with consistent properties, both mechanical and electrical. Thus, this reduces the number of particles which do not form usable agglomerates, for example, those which are too small to provide a conductive path through the carrier layer.
  • Figure 9
  • A diagrammatic illustration of conduction paths through a composite material in accordance with the invention is shown in Figure 9. In this example embodiment, the composite material has been incorporated into a touch screen having a deformable electrode of indium tin oxide (ITO) 901 and a rigid electrode of indium tin oxide (ITO) 902. A composite material 903 is sandwiched between the two electrodes 901 and 902, which comprises a solidified polymeric insulating carrier layer 904 and a plurality of agglomerates, such as agglomerate 905.
  • When a low force is applied to deformable electrode 901, indicated by arrow 906, agglomerate 905 is brought into contact with electrode 901 which creates a limited conduction path indicated by arrow 907, as shown in Figure 9A. In contrast, with respect to Figure 9B, when a larger force, indicated by arrow 908, is applied to electrode 901, contact is made, not only with agglomerate 905, but also agglomerates 909 and 910. Conduction paths are illustrated by arrows 911, 912 and 913. Thus, with increased force, contact is made with an increased number of agglomerates, thus increasing the conduction path. Furthermore, the agglomerates themselves may exhibit a pressure sensitive electrical resistance, such that with a higher applied force, there is also a further increase in conduction for this reason.
  • Figure 10
  • A graph of force against resistance for samples corresponding to composite materials of the type previously manufactured in accordance with the applicant's patent EP 2 689 431 , and composite materials in accordance with the present invention is shown in Figure 10.
  • Line 1001 shows the force-resistance response of a sample in accordance with the present invention, where the agglomerates have been pre-formed. Line 1002 shows the force-resistance response of a sample in accordance with the previously known method which creates agglomerates spontaneously. In the sample used here, the agglomerates were pre-formed using a centrifugal mixer as described with respect to Figure 3, at a rotational speed of 2000 rpm for four minutes.
  • It is noted that the present invention produces a less sensitive force-resistance response at low forces, meaning the composite material operates less like a switch than conventional methods. This can be useful in digital on/off applications. Visible light transmission is also improved as there is reduced haze from lack of non-conducting smaller agglomerates.
  • Thus, the present invention not only provides a suitable method for controlling the parameters of the agglomerates to suit a particular application, but also provides characteristics that are not provided by spontaneous agglomerate formation.

Claims (14)

  1. A method of producing a plurality of agglomerates (102) for inclusion in an electrically responsive composite material (101), comprising the steps of:
    obtaining a plurality of electrically conductive or semi-conductive particles (103);
    mixing said plurality of electrically conductive or semi-conductive particles in a centrifugal mixer (202), said mixing step comprising operating said centrifugal mixer at a Froude number of between 220 and 1100; and
    adhering said plurality of electrically conductive or semi-conductive particles by adding a granulation binder (203) and mixing said granulation binder with said plurality of electrically conductive or semi-conductive particles to form a plurality of agglomerates; characterised in that:
    each said step of obtaining, mixing and adhering said electrically conductive or semi-conductive particles pre-forms said plurality of agglomerates prior to introduction of said plurality of agglomerates into said electrically responsive composite material.
  2. The method of producing a plurality of agglomerates according to claim 1, further comprising the step of: performing a size selection process to ensure each said agglomerate is within a predetermined size range.
  3. The method of producing a plurality of agglomerates according to claim 2, wherein said size selection process comprises sieving.
  4. The method of producing a plurality of agglomerates according to any one of claims 1 to 3, further comprising the step of curing each said agglomerate by a heating process.
  5. A method of producing a composite material, comprising the steps of:
    obtaining a plurality of agglomerates (102);
    introducing said plurality of agglomerates into a liquid carrier comprising a component capable of solidifying to produce a solidified polymeric material; and
    mixing said plurality of agglomerates into said liquid carrier to produce a composite material; wherein each said agglomerate is pre-formed by the method of claim 1.
  6. The method of producing a composite material according to claim 5, wherein said centrifugal mixer has a dual axis of rotation.
  7. The method of producing a composite material according to claim 6, wherein said centrifugal mixer is rotated at a speed of between 1000 and 3500 rpm.
  8. The method of producing a composite material according to any of claims 5 to 7, wherein said granulation binder is added at a ratio of said plurality of electrically conductive or semi-conductive particles to binder of 10:1 weight/weight.
  9. The method of producing a composite material according to any one of claims 5 to 8, wherein said granulation binder comprises a silicone liquid binder.
  10. The method of producing a composite material according to claim 5, wherein each said agglomerate (601, 602) comprises a surface (605) having a plurality of indentations (603, 604) and has a largest dimension of more than 40 micrometres.
  11. The method of producing a composite material according to claim 5, wherein each said agglomerate has a largest dimension of between 4 and 20 micrometres.
  12. The method of producing a composite material according to claim 11, wherein each said agglomerate has a largest dimension of between 4 and 10 micrometres.
  13. The method of producing a composite material according to any one of claims 5 to 12, wherein said plurality of electrically conductive or semi-conductive particles comprise antimony doped tin oxide spherical particles.
  14. The method of producing a composite material according to any one of claims 5 to 13, wherein each said electrically conductive or semi-conductive particle has a largest dimension of between 10 and 100 nanometres.
EP18721091.9A 2017-04-21 2018-04-18 Method of producing agglomerates for inclusion in a composite material Active EP3612376B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB1706363.7A GB2561609B (en) 2017-04-21 2017-04-21 Method of producing agglomerates for inclusion in a composite material
PCT/GB2018/000069 WO2018193222A1 (en) 2017-04-21 2018-04-18 Composite material

Publications (2)

Publication Number Publication Date
EP3612376A1 EP3612376A1 (en) 2020-02-26
EP3612376B1 true EP3612376B1 (en) 2021-10-06

Family

ID=58795705

Family Applications (1)

Application Number Title Priority Date Filing Date
EP18721091.9A Active EP3612376B1 (en) 2017-04-21 2018-04-18 Method of producing agglomerates for inclusion in a composite material

Country Status (7)

Country Link
US (1) US20210147638A1 (en)
EP (1) EP3612376B1 (en)
JP (1) JP2020519704A (en)
KR (1) KR20190141716A (en)
CN (1) CN110536791B (en)
GB (1) GB2561609B (en)
WO (1) WO2018193222A1 (en)

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2457962A (en) * 1945-02-19 1949-01-04 Phillips Petroleum Co Agglomeration of powdered material
JPS5273399A (en) * 1975-12-17 1977-06-20 Inoue Japax Res Pressure sensing resistor
US4745301A (en) * 1985-12-13 1988-05-17 Advanced Micro-Matrix, Inc. Pressure sensitive electro-conductive materials
EP0231068B1 (en) * 1986-01-14 1994-03-16 RAYCHEM CORPORATION (a Delaware corporation) Conductive polymer composition
TW277152B (en) * 1994-05-10 1996-06-01 Hitachi Chemical Co Ltd
AU2176899A (en) * 1998-01-23 1999-08-09 Peratech Ltd Polymer composition
CN101496113A (en) * 2006-07-29 2009-07-29 肖克科技有限公司 Voltage switchable dielectric material having high aspect ratio particles
US8197719B2 (en) * 2006-11-17 2012-06-12 American Lithium Energy Corp. Electroactive agglomerated particles
GB0815724D0 (en) * 2008-08-29 2008-10-08 Peratech Ltd Pressure sensitive composition
CA2807691C (en) * 2010-08-11 2019-02-26 Timcal S.A. Ground expanded graphite agglomerates, methods of making, and applications of the same
KR101345694B1 (en) * 2011-03-11 2013-12-30 옵토팩 주식회사 Fiber, Fiber aggregate and Adhesive having the same
GB201105025D0 (en) * 2011-03-25 2011-05-11 Peratech Ltd Electrically responsive composite material
WO2014087984A1 (en) * 2012-12-06 2014-06-12 積水化学工業株式会社 Organic-inorganic hybrid particles, conductive particles, conductive material and connection structure
JP6262503B2 (en) * 2013-11-26 2018-01-17 三星電子株式会社Samsung Electronics Co.,Ltd. All-solid secondary battery and method for producing all-solid secondary battery
WO2015135463A1 (en) * 2014-03-11 2015-09-17 The Hong Kong University Of Science And Technology Electrical and thermal conductive paste composition and method of reducing percolation threshold and enhancing percolating conductivity using the same
CN105185469B (en) * 2015-09-23 2017-04-19 彩虹集团电子股份有限公司 Preparation method of high-stability conductive silver paste used for touch screen

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
EP3612376A1 (en) 2020-02-26
JP2020519704A (en) 2020-07-02
WO2018193222A1 (en) 2018-10-25
CN110536791B (en) 2021-10-15
GB2561609A (en) 2018-10-24
CN110536791A (en) 2019-12-03
KR20190141716A (en) 2019-12-24
GB2561609B (en) 2019-12-18
GB201706363D0 (en) 2017-06-07
US20210147638A1 (en) 2021-05-20

Similar Documents

Publication Publication Date Title
Wang et al. Effect of lubricant viscosity on the self-healing properties and electrically driven sliding of droplets on anisotropic slippery surfaces
CN106768520B (en) Pressure sensor and preparation method thereof
KR101980388B1 (en) Pressure sensitive polymer composite material adapted for touch screen
JP5337694B2 (en) Particles for use in electrophoretic displays
US20080303778A1 (en) Image display medium, image display device, storage medium storing an image display program, and image display method
Park et al. How the interaction between styrene-butadiene-rubber (SBR) binder and a secondary fluid affects the rheology, microstructure and adhesive properties of capillary-suspension-type graphite slurries used for Li-ion battery anodes
TW201213996A (en) Particles for image display, production method thereof, electrophoretic dispersion liquid, and image display device
EP2578639B1 (en) Resin blend for melt-processing, pellet, method for manufacturing resin-molded product using same and resin-molded product
EP3612376B1 (en) Method of producing agglomerates for inclusion in a composite material
Yabu Fabrication of nanostructured composite microspheres based on the self‐assembly of polymers and functional nanomaterials
JP2000297122A (en) Polymer particle
JP5313388B2 (en) Switchable particle-based display and manufacturing method thereof
US10208252B2 (en) Ethylene-vinyl acetate copolymer, liquid crystal film layer, display panel and preparing method thereof
GB2505035A (en) Isotropic conductive adhesive
Wu et al. Molecular investigation of adsorption behaviors of hydroxyl-terminated polybutadiene (HTPB) binders onto copper surface: The effects of aluminum nanoparticles
Taning et al. Characterization of solvent-dependent ink structure and catalyst layer morphology based on ink sedimentation dynamics and catalyst-ionomer cast films
KR20110136144A (en) Printing paste composition for electrode of touch panel and electrode forming method using the same
WO2023109595A1 (en) Inkjet printable ionic ink, ionic membrane and ionic tactile sensor
CN105907018A (en) Flexible thin film heating material and preparation method thereof
US20160060467A1 (en) Formulation and method for fabricating a transparent force sensing layer
Nam et al. Development and Characteristics of Multipurpose Transparent Polyurethane Film
Ávila et al. A nano-modified superhydrophobic membrane
Zhang Progress in preparation of monodisperse polymer microspheres
Pal et al. Design and fabrication of thin polymer coating on cotton fabric surface to impart hydrophobicity: An admicellar polymerization approach
US20110063196A1 (en) Electronic paper display device and manufacturing method thereof

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20191018

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20201022

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: B29C 67/24 20060101AFI20210429BHEP

Ipc: H01B 1/20 20060101ALI20210429BHEP

Ipc: B29K 505/06 20060101ALN20210429BHEP

INTG Intention to grant announced

Effective date: 20210514

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1435852

Country of ref document: AT

Kind code of ref document: T

Effective date: 20211015

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602018024630

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20211006

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1435852

Country of ref document: AT

Kind code of ref document: T

Effective date: 20211006

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220106

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220206

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220207

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220106

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220107

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602018024630

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20220707

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602018024630

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20220430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220418

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20221103

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220418

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211006